2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester

Base Information

Chemical Name:2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester
CAS No.:1186219-24-8
Molecular Formula:C₂₁H₂₂BrNO₄S
Molecular Weight:464.38
Hs Code.:

Synonyms:2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester

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Technology Process of 2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester

There total 1 articles about 2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

: 2462-31-9
benzyl 2-aminoacetate hydrochloride

: 196394-94-2
2-(acetylsulfanylmethyl)-3-(4-bromophenyl)propionic acid

: 1186219-24-8
2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester

Guidance literature:: With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; at 0 - 20 ℃;
DOI:10.1002/jlcr.1566

Reference yield:

: 1186219-24-8
2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester

: 1186219-26-0
2-[3-(4-bromophenyl)-2-(sulfanylmethyl)propionylamino]acetic acid disulfide

Guidance literature:: 2-[3-(4-bromophenyl)-2-(S-acetylsulfanylmethyl)propionylamino]acetic acid benzyl ester; With sodium hydroxide; In methanol; at 0 - 20 ℃; for 6.5h;

With iodine; In methanol; at 0 ℃; for 0.583333h;
DOI:10.1002/jlcr.1566